sx20 Search Results


sx20  (Applied Photophysics)
99
Applied Photophysics sx20
Sx20, supplied by Applied Photophysics, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/sx20/product/Applied Photophysics
Average 99 stars, based on 1 article reviews
sx20 - by Bioz Stars, 2026-01
99/100 stars
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sx20 led  (Applied Photophysics)
93
Applied Photophysics sx20 led
Sx20 Led, supplied by Applied Photophysics, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
sx20 led - by Bioz Stars, 2026-01
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photo-micrographed using a canon sx20 camera  (Canon inc)
90
Canon inc photo-micrographed using a canon sx20 camera
Photo Micrographed Using A Canon Sx20 Camera, supplied by Canon inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
photo-micrographed using a canon sx20 camera - by Bioz Stars, 2026-01
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scintillation liquid sx20-5  (Fisher Scientific)
90
Fisher Scientific scintillation liquid sx20-5
(A) Human fetal RPE (fRPE) cultures were treated with either transferrin-bound ferric iron (Tf· 55 Fe 3+ ) or ferrous iron ascorbate ( 55 Fe 2+ ) alone or in the presence of recombinant IL-1β (rIL-1β). Intracellular iron accumulation in fRPE lysates was measured during 8 h of treatment using a <t>scintillation</t> counter to quantify counts per minute (CPM) (n = 3/group). (B) fRPE cultures were treated with either media (vehicle) or recombinant IL-1β (rIL-1β) for 8 h before cells were harvested for qPCR analysis of iron transport/ regulatory genes (n = 6/group). (C) Mass in grams of WT and Il1b −/− (KO) mice fed an LFD or an HFD (n = 20/group). (D) VAT and SAT hypertrophy were dependent on diet but not genotype (n = 10/group). (E) Diet and genotype had no effect on glycemic control measured with intraperitoneal glucose tolerance test (n = 10/group). (F) RPE gene expression measured by qPCR following 12 weeks of either LFD or HFD (n = 5/group). (G) Retinal CD11b + cell gene expression following 12 weeks of either LFD or HFD (n = 5/group). (H) HFD WT mice accumulate RPE iron, measured using inductively coupled plasma mass spectrometry, which is rescued in the HFD Il1b −/− mice (n = 10/group). (I) HFD WT mice accumulate lipid oxidation product MDA in RPE, which is rescued in HFD Il1b −/− mice (n = 10/group). (J) HFD WT mice RPE upregulate Hmox1 in an Il1b -dependent manner (n = 5/group). (K) HFD WT mice exhibit c-wave amplitude deficits, measured by electroretinography, which is rescued in HFD Il1b −/− mice (n = 10/group). Data indicate mean and, where error bars are shown, ± SD. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, by 1-way ANOVA with multiple comparisons (A), unpaired Student’s t test (B), or 2-way repeated-measures ANOVA (C and E) or 2-way ANOVA (D and F–K) with Tukey’s HSD post hoc test.
Scintillation Liquid Sx20 5, supplied by Fisher Scientific, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/scintillation liquid sx20-5/product/Fisher Scientific
Average 90 stars, based on 1 article reviews
scintillation liquid sx20-5 - by Bioz Stars, 2026-01
90/100 stars
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lerite sx 20  (SEPPIC Inc)
90
SEPPIC Inc lerite sx 20
(A) Human fetal RPE (fRPE) cultures were treated with either transferrin-bound ferric iron (Tf· 55 Fe 3+ ) or ferrous iron ascorbate ( 55 Fe 2+ ) alone or in the presence of recombinant IL-1β (rIL-1β). Intracellular iron accumulation in fRPE lysates was measured during 8 h of treatment using a <t>scintillation</t> counter to quantify counts per minute (CPM) (n = 3/group). (B) fRPE cultures were treated with either media (vehicle) or recombinant IL-1β (rIL-1β) for 8 h before cells were harvested for qPCR analysis of iron transport/ regulatory genes (n = 6/group). (C) Mass in grams of WT and Il1b −/− (KO) mice fed an LFD or an HFD (n = 20/group). (D) VAT and SAT hypertrophy were dependent on diet but not genotype (n = 10/group). (E) Diet and genotype had no effect on glycemic control measured with intraperitoneal glucose tolerance test (n = 10/group). (F) RPE gene expression measured by qPCR following 12 weeks of either LFD or HFD (n = 5/group). (G) Retinal CD11b + cell gene expression following 12 weeks of either LFD or HFD (n = 5/group). (H) HFD WT mice accumulate RPE iron, measured using inductively coupled plasma mass spectrometry, which is rescued in the HFD Il1b −/− mice (n = 10/group). (I) HFD WT mice accumulate lipid oxidation product MDA in RPE, which is rescued in HFD Il1b −/− mice (n = 10/group). (J) HFD WT mice RPE upregulate Hmox1 in an Il1b -dependent manner (n = 5/group). (K) HFD WT mice exhibit c-wave amplitude deficits, measured by electroretinography, which is rescued in HFD Il1b −/− mice (n = 10/group). Data indicate mean and, where error bars are shown, ± SD. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, by 1-way ANOVA with multiple comparisons (A), unpaired Student’s t test (B), or 2-way repeated-measures ANOVA (C and E) or 2-way ANOVA (D and F–K) with Tukey’s HSD post hoc test.
Lerite Sx 20, supplied by SEPPIC Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lerite sx 20/product/SEPPIC Inc
Average 90 stars, based on 1 article reviews
lerite sx 20 - by Bioz Stars, 2026-01
90/100 stars
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sx20 spectrometer  (Coy Laboratory)
90
Coy Laboratory sx20 spectrometer
(A) Human fetal RPE (fRPE) cultures were treated with either transferrin-bound ferric iron (Tf· 55 Fe 3+ ) or ferrous iron ascorbate ( 55 Fe 2+ ) alone or in the presence of recombinant IL-1β (rIL-1β). Intracellular iron accumulation in fRPE lysates was measured during 8 h of treatment using a <t>scintillation</t> counter to quantify counts per minute (CPM) (n = 3/group). (B) fRPE cultures were treated with either media (vehicle) or recombinant IL-1β (rIL-1β) for 8 h before cells were harvested for qPCR analysis of iron transport/ regulatory genes (n = 6/group). (C) Mass in grams of WT and Il1b −/− (KO) mice fed an LFD or an HFD (n = 20/group). (D) VAT and SAT hypertrophy were dependent on diet but not genotype (n = 10/group). (E) Diet and genotype had no effect on glycemic control measured with intraperitoneal glucose tolerance test (n = 10/group). (F) RPE gene expression measured by qPCR following 12 weeks of either LFD or HFD (n = 5/group). (G) Retinal CD11b + cell gene expression following 12 weeks of either LFD or HFD (n = 5/group). (H) HFD WT mice accumulate RPE iron, measured using inductively coupled plasma mass spectrometry, which is rescued in the HFD Il1b −/− mice (n = 10/group). (I) HFD WT mice accumulate lipid oxidation product MDA in RPE, which is rescued in HFD Il1b −/− mice (n = 10/group). (J) HFD WT mice RPE upregulate Hmox1 in an Il1b -dependent manner (n = 5/group). (K) HFD WT mice exhibit c-wave amplitude deficits, measured by electroretinography, which is rescued in HFD Il1b −/− mice (n = 10/group). Data indicate mean and, where error bars are shown, ± SD. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, by 1-way ANOVA with multiple comparisons (A), unpaired Student’s t test (B), or 2-way repeated-measures ANOVA (C and E) or 2-way ANOVA (D and F–K) with Tukey’s HSD post hoc test.
Sx20 Spectrometer, supplied by Coy Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
sx20 spectrometer - by Bioz Stars, 2026-01
90/100 stars
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Image Search Results


(A) Human fetal RPE (fRPE) cultures were treated with either transferrin-bound ferric iron (Tf· 55 Fe 3+ ) or ferrous iron ascorbate ( 55 Fe 2+ ) alone or in the presence of recombinant IL-1β (rIL-1β). Intracellular iron accumulation in fRPE lysates was measured during 8 h of treatment using a scintillation counter to quantify counts per minute (CPM) (n = 3/group). (B) fRPE cultures were treated with either media (vehicle) or recombinant IL-1β (rIL-1β) for 8 h before cells were harvested for qPCR analysis of iron transport/ regulatory genes (n = 6/group). (C) Mass in grams of WT and Il1b −/− (KO) mice fed an LFD or an HFD (n = 20/group). (D) VAT and SAT hypertrophy were dependent on diet but not genotype (n = 10/group). (E) Diet and genotype had no effect on glycemic control measured with intraperitoneal glucose tolerance test (n = 10/group). (F) RPE gene expression measured by qPCR following 12 weeks of either LFD or HFD (n = 5/group). (G) Retinal CD11b + cell gene expression following 12 weeks of either LFD or HFD (n = 5/group). (H) HFD WT mice accumulate RPE iron, measured using inductively coupled plasma mass spectrometry, which is rescued in the HFD Il1b −/− mice (n = 10/group). (I) HFD WT mice accumulate lipid oxidation product MDA in RPE, which is rescued in HFD Il1b −/− mice (n = 10/group). (J) HFD WT mice RPE upregulate Hmox1 in an Il1b -dependent manner (n = 5/group). (K) HFD WT mice exhibit c-wave amplitude deficits, measured by electroretinography, which is rescued in HFD Il1b −/− mice (n = 10/group). Data indicate mean and, where error bars are shown, ± SD. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, by 1-way ANOVA with multiple comparisons (A), unpaired Student’s t test (B), or 2-way repeated-measures ANOVA (C and E) or 2-way ANOVA (D and F–K) with Tukey’s HSD post hoc test.

Journal: Cell reports

Article Title: Inflammatory adipose activates a nutritional immunity pathway leading to retinal dysfunction

doi: 10.1016/j.celrep.2022.110942

Figure Lengend Snippet: (A) Human fetal RPE (fRPE) cultures were treated with either transferrin-bound ferric iron (Tf· 55 Fe 3+ ) or ferrous iron ascorbate ( 55 Fe 2+ ) alone or in the presence of recombinant IL-1β (rIL-1β). Intracellular iron accumulation in fRPE lysates was measured during 8 h of treatment using a scintillation counter to quantify counts per minute (CPM) (n = 3/group). (B) fRPE cultures were treated with either media (vehicle) or recombinant IL-1β (rIL-1β) for 8 h before cells were harvested for qPCR analysis of iron transport/ regulatory genes (n = 6/group). (C) Mass in grams of WT and Il1b −/− (KO) mice fed an LFD or an HFD (n = 20/group). (D) VAT and SAT hypertrophy were dependent on diet but not genotype (n = 10/group). (E) Diet and genotype had no effect on glycemic control measured with intraperitoneal glucose tolerance test (n = 10/group). (F) RPE gene expression measured by qPCR following 12 weeks of either LFD or HFD (n = 5/group). (G) Retinal CD11b + cell gene expression following 12 weeks of either LFD or HFD (n = 5/group). (H) HFD WT mice accumulate RPE iron, measured using inductively coupled plasma mass spectrometry, which is rescued in the HFD Il1b −/− mice (n = 10/group). (I) HFD WT mice accumulate lipid oxidation product MDA in RPE, which is rescued in HFD Il1b −/− mice (n = 10/group). (J) HFD WT mice RPE upregulate Hmox1 in an Il1b -dependent manner (n = 5/group). (K) HFD WT mice exhibit c-wave amplitude deficits, measured by electroretinography, which is rescued in HFD Il1b −/− mice (n = 10/group). Data indicate mean and, where error bars are shown, ± SD. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, by 1-way ANOVA with multiple comparisons (A), unpaired Student’s t test (B), or 2-way repeated-measures ANOVA (C and E) or 2-way ANOVA (D and F–K) with Tukey’s HSD post hoc test.

Article Snippet: 100ul of the cell lysate was added to a scintillation tube with 1mL of scintillation liquid (Catalog #: SX20-5, Fisher Scientific, Pittsburgh, PA, USA).

Techniques: Recombinant, Control, Gene Expression, Clinical Proteomics, Mass Spectrometry